SREB, a GATA transcription factor that directs disparate fates in Blastomyces dermatitidis including morphogenesis and siderophore biosynthesis.

Blastomyces dermatitidis belongs to a group of human pathogenic fungi that exhibit thermal dimorphism. At 22 degrees C, these fungi grow as mold that produce conidia or infectious particles, whereas at 37 degrees C they convert to budding yeast. The ability to switch between these forms is essential...

Full description

Bibliographic Details
Main Authors: Gregory M Gauthier, Thomas D Sullivan, Sergio S Gallardo, T Tristan Brandhorst, Amber J Vanden Wymelenberg, Christina A Cuomo, Garret Suen, Cameron R Currie, Bruce S Klein
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2010-04-01
Series:PLoS Pathogens
Online Access:http://europepmc.org/articles/PMC2848559?pdf=render
_version_ 1818359347284017152
author Gregory M Gauthier
Thomas D Sullivan
Sergio S Gallardo
T Tristan Brandhorst
Amber J Vanden Wymelenberg
Christina A Cuomo
Garret Suen
Cameron R Currie
Bruce S Klein
author_facet Gregory M Gauthier
Thomas D Sullivan
Sergio S Gallardo
T Tristan Brandhorst
Amber J Vanden Wymelenberg
Christina A Cuomo
Garret Suen
Cameron R Currie
Bruce S Klein
author_sort Gregory M Gauthier
collection DOAJ
description Blastomyces dermatitidis belongs to a group of human pathogenic fungi that exhibit thermal dimorphism. At 22 degrees C, these fungi grow as mold that produce conidia or infectious particles, whereas at 37 degrees C they convert to budding yeast. The ability to switch between these forms is essential for virulence in mammals and may enable these organisms to survive in the soil. To identify genes that regulate this phase transition, we used Agrobacterium tumefaciens to mutagenize B. dermatitidis conidia and screened transformants for defects in morphogenesis. We found that the GATA transcription factor SREB governs multiple fates in B. dermatitidis: phase transition from yeast to mold, cell growth at 22 degrees C, and biosynthesis of siderophores under iron-replete conditions. Insertional and null mutants fail to convert to mold, do not accumulate significant biomass at 22 degrees C, and are unable to suppress siderophore biosynthesis under iron-replete conditions. The defect in morphogenesis in the SREB mutant was independent of exogenous iron concentration, suggesting that SREB promotes the phase transition by altering the expression of genes that are unrelated to siderophore biosynthesis. Using bioinformatic and gene expression analyses, we identified candidate genes with upstream GATA sites whose expression is altered in the null mutant that may be direct or indirect targets of SREB and promote the phase transition. We conclude that SREB functions as a transcription factor that promotes morphogenesis and regulates siderophore biosynthesis. To our knowledge, this is the first gene identified that promotes the conversion from yeast to mold in the dimorphic fungi, and may shed light on environmental persistence of these pathogens.
first_indexed 2024-12-13T20:43:27Z
format Article
id doaj.art-50fdfe58eadd4c268b5e500f0cdec7de
institution Directory Open Access Journal
issn 1553-7366
1553-7374
language English
last_indexed 2024-12-13T20:43:27Z
publishDate 2010-04-01
publisher Public Library of Science (PLoS)
record_format Article
series PLoS Pathogens
spelling doaj.art-50fdfe58eadd4c268b5e500f0cdec7de2022-12-21T23:32:05ZengPublic Library of Science (PLoS)PLoS Pathogens1553-73661553-73742010-04-0164e100084610.1371/journal.ppat.1000846SREB, a GATA transcription factor that directs disparate fates in Blastomyces dermatitidis including morphogenesis and siderophore biosynthesis.Gregory M GauthierThomas D SullivanSergio S GallardoT Tristan BrandhorstAmber J Vanden WymelenbergChristina A CuomoGarret SuenCameron R CurrieBruce S KleinBlastomyces dermatitidis belongs to a group of human pathogenic fungi that exhibit thermal dimorphism. At 22 degrees C, these fungi grow as mold that produce conidia or infectious particles, whereas at 37 degrees C they convert to budding yeast. The ability to switch between these forms is essential for virulence in mammals and may enable these organisms to survive in the soil. To identify genes that regulate this phase transition, we used Agrobacterium tumefaciens to mutagenize B. dermatitidis conidia and screened transformants for defects in morphogenesis. We found that the GATA transcription factor SREB governs multiple fates in B. dermatitidis: phase transition from yeast to mold, cell growth at 22 degrees C, and biosynthesis of siderophores under iron-replete conditions. Insertional and null mutants fail to convert to mold, do not accumulate significant biomass at 22 degrees C, and are unable to suppress siderophore biosynthesis under iron-replete conditions. The defect in morphogenesis in the SREB mutant was independent of exogenous iron concentration, suggesting that SREB promotes the phase transition by altering the expression of genes that are unrelated to siderophore biosynthesis. Using bioinformatic and gene expression analyses, we identified candidate genes with upstream GATA sites whose expression is altered in the null mutant that may be direct or indirect targets of SREB and promote the phase transition. We conclude that SREB functions as a transcription factor that promotes morphogenesis and regulates siderophore biosynthesis. To our knowledge, this is the first gene identified that promotes the conversion from yeast to mold in the dimorphic fungi, and may shed light on environmental persistence of these pathogens.http://europepmc.org/articles/PMC2848559?pdf=render
spellingShingle Gregory M Gauthier
Thomas D Sullivan
Sergio S Gallardo
T Tristan Brandhorst
Amber J Vanden Wymelenberg
Christina A Cuomo
Garret Suen
Cameron R Currie
Bruce S Klein
SREB, a GATA transcription factor that directs disparate fates in Blastomyces dermatitidis including morphogenesis and siderophore biosynthesis.
PLoS Pathogens
title SREB, a GATA transcription factor that directs disparate fates in Blastomyces dermatitidis including morphogenesis and siderophore biosynthesis.
title_full SREB, a GATA transcription factor that directs disparate fates in Blastomyces dermatitidis including morphogenesis and siderophore biosynthesis.
title_fullStr SREB, a GATA transcription factor that directs disparate fates in Blastomyces dermatitidis including morphogenesis and siderophore biosynthesis.
title_full_unstemmed SREB, a GATA transcription factor that directs disparate fates in Blastomyces dermatitidis including morphogenesis and siderophore biosynthesis.
title_short SREB, a GATA transcription factor that directs disparate fates in Blastomyces dermatitidis including morphogenesis and siderophore biosynthesis.
title_sort sreb a gata transcription factor that directs disparate fates in blastomyces dermatitidis including morphogenesis and siderophore biosynthesis
url http://europepmc.org/articles/PMC2848559?pdf=render
work_keys_str_mv AT gregorymgauthier srebagatatranscriptionfactorthatdirectsdisparatefatesinblastomycesdermatitidisincludingmorphogenesisandsiderophorebiosynthesis
AT thomasdsullivan srebagatatranscriptionfactorthatdirectsdisparatefatesinblastomycesdermatitidisincludingmorphogenesisandsiderophorebiosynthesis
AT sergiosgallardo srebagatatranscriptionfactorthatdirectsdisparatefatesinblastomycesdermatitidisincludingmorphogenesisandsiderophorebiosynthesis
AT ttristanbrandhorst srebagatatranscriptionfactorthatdirectsdisparatefatesinblastomycesdermatitidisincludingmorphogenesisandsiderophorebiosynthesis
AT amberjvandenwymelenberg srebagatatranscriptionfactorthatdirectsdisparatefatesinblastomycesdermatitidisincludingmorphogenesisandsiderophorebiosynthesis
AT christinaacuomo srebagatatranscriptionfactorthatdirectsdisparatefatesinblastomycesdermatitidisincludingmorphogenesisandsiderophorebiosynthesis
AT garretsuen srebagatatranscriptionfactorthatdirectsdisparatefatesinblastomycesdermatitidisincludingmorphogenesisandsiderophorebiosynthesis
AT cameronrcurrie srebagatatranscriptionfactorthatdirectsdisparatefatesinblastomycesdermatitidisincludingmorphogenesisandsiderophorebiosynthesis
AT brucesklein srebagatatranscriptionfactorthatdirectsdisparatefatesinblastomycesdermatitidisincludingmorphogenesisandsiderophorebiosynthesis